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158579-82-9

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158579-82-9 Usage

Description

5-NITRO-2-(TRIFLUOROMETHOXY)ANILINE is a specialized chemical compound that features both nitro and trifluoromethoxy functional groups attached to an aniline base. It is often used in advanced organic synthesis procedures, typically as part of intermediary steps towards the formulation of more complex substances. The presence of fluorine atoms in the form of a trifluoromethoxy group exhibits unique reactivity patterns, making it valuable for certain types of chemical transformations. As with many nitro compounds, it is important to handle this substance with care, as it can present certain hazards under specific conditions. Like other anilines, this compound is a derivative of ammonia and can potentially form hazardous products if improperly mixed with certain other substances.

Uses

Used in Advanced Organic Synthesis:
5-NITRO-2-(TRIFLUOROMETHOXY)ANILINE is used as an intermediate in the synthesis of more complex substances, particularly in the field of organic chemistry. Its unique reactivity patterns, due to the presence of the trifluoromethoxy group, make it a valuable component in the creation of advanced chemical compounds.
Used in Chemical Transformations:
In the chemical industry, 5-NITRO-2-(TRIFLUOROMETHOXY)ANILINE is used as a reagent for certain types of chemical transformations. The fluorine atoms in the trifluoromethoxy group contribute to its unique reactivity, allowing for specific reactions that may not be possible with other compounds.
Used in Pharmaceutical Development:
5-NITRO-2-(TRIFLUOROMETHOXY)ANILINE may be used as a building block in the development of new pharmaceuticals. Its properties and reactivity can be harnessed to create novel drug candidates, potentially leading to the discovery of new treatments for various medical conditions.
Used in Material Science:
In the field of material science, 5-NITRO-2-(TRIFLUOROMETHOXY)ANILINE can be used to develop new materials with specific properties. Its unique chemical structure may contribute to the creation of materials with improved characteristics, such as enhanced stability or reactivity.
Used in Research and Development:
5-NITRO-2-(TRIFLUOROMETHOXY)ANILINE is also used in research and development settings, where scientists and chemists explore its potential applications and properties. This may include studying its reactivity, stability, and potential uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 158579-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,5,7 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 158579-82:
(8*1)+(7*5)+(6*8)+(5*5)+(4*7)+(3*9)+(2*8)+(1*2)=189
189 % 10 = 9
So 158579-82-9 is a valid CAS Registry Number.

158579-82-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Nitro-2-(trifluoromethoxy)aniline

1.2 Other means of identification

Product number -
Other names 2-trifluoromethoxy-5-nitroaniline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:158579-82-9 SDS

158579-82-9Relevant articles and documents

4-benzoyl isoxazoles derivatives and their use as herbicides

-

, (2008/06/13)

4-Benzoylisoxazole derivatives of the formula wherein R is H or an ester; R1is alkyl, haloalkyl or optionally substituted cycloalkyl; R2is halogen, optionally halogenated alkyl, alkenyl or alkynyl; alkyl substituted with one or more —OR5; —NO2, —CN, —CO2R5, —S(O)pR6, —O(CH2)mOR5, —COR5, —NR5R6, —N(R8)SOqR7, —CONR9R10or —OR51; or optionally substituted phenyl; R3is —S(O)qR7; X is —N(R8)—; n is 0, 1, 2, 3, or 4; R5, R51and R6are independently H; optionally halogenated alkyl, alkenyl or alkynyl; optionally substituted phenyl; or cycloalkyl; R7is optionally halogenated alkyl, alkenyl or alkynyl; cycloalkyl; optionally substituted phenyl; or optionally substituted amino; R8is H; optionally halogenated alkyl, alkenyl or alkynyl; cycloalkyl; optionally substituted phenyl; or alkoxy; m is 1, 2 or 3; p is 0, 1 or 2; q is 0 or 2; and their use as herbicides are described.

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